-
1
-
-
33646010905
-
Rett syndrome in Australia: a review of the epidemiology
-
Laurvick C.L., Klerk N., Bower C., Christodoulou J., Ravine D., Ellaway C., et al. Rett syndrome in Australia: a review of the epidemiology. J Pediatr 2006, 148:347-352.
-
(2006)
J Pediatr
, vol.148
, pp. 347-352
-
-
Laurvick, C.L.1
Klerk, N.2
Bower, C.3
Christodoulou, J.4
Ravine, D.5
Ellaway, C.6
-
2
-
-
0032830639
-
Rett syndrome is caused by mutations in x-linked MECP2 encoding methyl-CpG-binding protien 2
-
Amir R.E., Van Der Veyver I.B., Wan M., Tran C.Q., Francke U., Zoghbi H.U. Rett syndrome is caused by mutations in x-linked MECP2 encoding methyl-CpG-binding protien 2. Nat Genet 1999, 23:185-188.
-
(1999)
Nat Genet
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
Van Der Veyver, I.B.2
Wan, M.3
Tran, C.Q.4
Francke, U.5
Zoghbi, H.U.6
-
3
-
-
42249095974
-
Specific mutations in Methyl-CpG-Binding Protien 2 confer different severity in Rett syndrome
-
Neul J.L. Specific mutations in Methyl-CpG-Binding Protien 2 confer different severity in Rett syndrome. Neurology 2008, 70:1313-1321.
-
(2008)
Neurology
, vol.70
, pp. 1313-1321
-
-
Neul, J.L.1
-
4
-
-
40549110266
-
Investigating the genotype phenotype relationship in Rett syndrome using an international data set
-
Bebbington A., Anderson A., Ravine D., Fyfe S., Pineda M., Klerk N., et al. Investigating the genotype phenotype relationship in Rett syndrome using an international data set. Neurology 2008, 70:868-875.
-
(2008)
Neurology
, vol.70
, pp. 868-875
-
-
Bebbington, A.1
Anderson, A.2
Ravine, D.3
Fyfe, S.4
Pineda, M.5
Klerk, N.6
-
5
-
-
37349125534
-
Feeding experiences and growth status in a Rett syndrome population
-
Oddy W., Webb K., Baikie G., Thompson S., Reilly S., Fyfe S., et al. Feeding experiences and growth status in a Rett syndrome population. J Pediatr Gastroenterol Nutr 2007, 45:582-590.
-
(2007)
J Pediatr Gastroenterol Nutr
, vol.45
, pp. 582-590
-
-
Oddy, W.1
Webb, K.2
Baikie, G.3
Thompson, S.4
Reilly, S.5
Fyfe, S.6
-
6
-
-
0035835984
-
Growth and nutrition in Rett syndrome
-
Reilly S., Cass H. Growth and nutrition in Rett syndrome. Disabil Rehabil 2001, 23:118-128.
-
(2001)
Disabil Rehabil
, vol.23
, pp. 118-128
-
-
Reilly, S.1
Cass, H.2
-
7
-
-
0026712191
-
Growth and nutrition in 10 girls with Rett syndrome
-
Thommessen M., Kase B., Heiberg A. Growth and nutrition in 10 girls with Rett syndrome. Acta Paediatr 1992, 81:686-690.
-
(1992)
Acta Paediatr
, vol.81
, pp. 686-690
-
-
Thommessen, M.1
Kase, B.2
Heiberg, A.3
-
8
-
-
0033548615
-
Metacarpophalangeal pattern profile and bone age in Rett syndrome: further radiological clues to the diagnosis
-
Leonard H., Thomson M., Glasson E., Fyfe S., Leonard S., Ellaway C., et al. Metacarpophalangeal pattern profile and bone age in Rett syndrome: further radiological clues to the diagnosis. Am J Med Genet 1999, 83:88-95.
-
(1999)
Am J Med Genet
, vol.83
, pp. 88-95
-
-
Leonard, H.1
Thomson, M.2
Glasson, E.3
Fyfe, S.4
Leonard, S.5
Ellaway, C.6
-
9
-
-
0032940559
-
A population based approach to the investigation of osteopenia in Rett syndrome
-
Leonard H., Thomson M., Glasson E., Fyfe S., Leonard S., Bower C., et al. A population based approach to the investigation of osteopenia in Rett syndrome. Dev Med Child Neurol 1999, 41:323-328.
-
(1999)
Dev Med Child Neurol
, vol.41
, pp. 323-328
-
-
Leonard, H.1
Thomson, M.2
Glasson, E.3
Fyfe, S.4
Leonard, S.5
Bower, C.6
-
10
-
-
0029111619
-
Skeletal abnormalities in Rett syndrome: increasing evidence for dysmorphogenetic defects
-
Leonard H., Thomson M., Bower C., Fyfe S., Constantinou J. Skeletal abnormalities in Rett syndrome: increasing evidence for dysmorphogenetic defects. Am J Med Genet 1995, 58:282-285.
-
(1995)
Am J Med Genet
, vol.58
, pp. 282-285
-
-
Leonard, H.1
Thomson, M.2
Bower, C.3
Fyfe, S.4
Constantinou, J.5
-
11
-
-
79952372107
-
Bone mineral content and density in Rett syndrome and their contributing factors
-
Jefferson A., Woodhead H.J., Fyfe S., Briody J., Bebbington A., Strauss B.J., et al. Bone mineral content and density in Rett syndrome and their contributing factors. Pediatr Res 2011, 69:293-298.
-
(2011)
Pediatr Res
, vol.69
, pp. 293-298
-
-
Jefferson, A.1
Woodhead, H.J.2
Fyfe, S.3
Briody, J.4
Bebbington, A.5
Strauss, B.J.6
-
12
-
-
0035210806
-
Endocrinological study on growth retardation in Rett syndrome
-
Huppke P., Roth C., Christen H., Brockmann K., Hanefeld F. Endocrinological study on growth retardation in Rett syndrome. Acta Paediatr 2001, 90:1257-1261.
-
(2001)
Acta Paediatr
, vol.90
, pp. 1257-1261
-
-
Huppke, P.1
Roth, C.2
Christen, H.3
Brockmann, K.4
Hanefeld, F.5
-
13
-
-
55049114903
-
Bone mineral content and bone mineral density are lower in older than in younger females with Rett syndrome
-
Motil K.J., Ellis K.J., Barrish J.O., Caeg E., Glaze D.G. Bone mineral content and bone mineral density are lower in older than in younger females with Rett syndrome. Pediatr Res 2008, 64:435-439.
-
(2008)
Pediatr Res
, vol.64
, pp. 435-439
-
-
Motil, K.J.1
Ellis, K.J.2
Barrish, J.O.3
Caeg, E.4
Glaze, D.G.5
-
14
-
-
80051987666
-
DXA measurements in Rett syndrome reveal small bones with low bone mass
-
Roende G., Ravn K., Fuglsang K., Andersen H., Bieber Nielsen J., Brøndum-Nielsen K., et al. DXA measurements in Rett syndrome reveal small bones with low bone mass. J Bone Miner Res 2011, 26:2280-2286.
-
(2011)
J Bone Miner Res
, vol.26
, pp. 2280-2286
-
-
Roende, G.1
Ravn, K.2
Fuglsang, K.3
Andersen, H.4
Bieber Nielsen, J.5
Brøndum-Nielsen, K.6
-
15
-
-
0033024279
-
Organ growth in Rett syndrome: a postmortem examination analysis
-
Armstrong D.D., Dunn J.K., Schultz R.J., Herbert D.A., Glaze D.G., Motil K.J. Organ growth in Rett syndrome: a postmortem examination analysis. Pediatr Neurol 1999, 20:125-129.
-
(1999)
Pediatr Neurol
, vol.20
, pp. 125-129
-
-
Armstrong, D.D.1
Dunn, J.K.2
Schultz, R.J.3
Herbert, D.A.4
Glaze, D.G.5
Motil, K.J.6
-
16
-
-
0031978042
-
Hand and foot growth failure in Rett syndrome
-
Schultz R., Glaze D., Motil K., Hebert D., Percy A. Hand and foot growth failure in Rett syndrome. J Child Neurol 1998, 13:71-74.
-
(1998)
J Child Neurol
, vol.13
, pp. 71-74
-
-
Schultz, R.1
Glaze, D.2
Motil, K.3
Hebert, D.4
Percy, A.5
-
18
-
-
0031757555
-
Diagnosis of Rett syndrome: can a radiograph help
-
Glasson E., Bower C., Thomson M., Fyfe S., Leonard S., Rousham B., et al. Diagnosis of Rett syndrome: can a radiograph help. Dev Med Child Neurol 1998, 40:737-742.
-
(1998)
Dev Med Child Neurol
, vol.40
, pp. 737-742
-
-
Glasson, E.1
Bower, C.2
Thomson, M.3
Fyfe, S.4
Leonard, S.5
Rousham, B.6
-
19
-
-
40949158036
-
Early determinents of fractures in Rett syndrome
-
Downs J., Bebbington A., Woodhead H., Jacoby P., Jian L., Jefferson A., et al. Early determinents of fractures in Rett syndrome. Pediatrics 2008, 121:540-546.
-
(2008)
Pediatrics
, vol.121
, pp. 540-546
-
-
Downs, J.1
Bebbington, A.2
Woodhead, H.3
Jacoby, P.4
Jian, L.5
Jefferson, A.6
-
20
-
-
77953533210
-
Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development
-
Alvarez-Saavedra M., Carrasco L., Sura-Trueba S., Aiello V.D., Walz K., Neto J.X., et al. Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development. Hum Mol Genet 2010, 19:2177-2190.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 2177-2190
-
-
Alvarez-Saavedra, M.1
Carrasco, L.2
Sura-Trueba, S.3
Aiello, V.D.4
Walz, K.5
Neto, J.X.6
-
21
-
-
79961162133
-
IUGR differentially alters MeCP2 expression and H3K9Me3 of the PPARgamma gene in male and female rat lungs during alveolarization
-
Joss-Moore L.A., Wang Y., Ogata E.M., Sainz A.J., Yu X., Callaway C.W., et al. IUGR differentially alters MeCP2 expression and H3K9Me3 of the PPARgamma gene in male and female rat lungs during alveolarization. Birt Defects Res A Clin Mol Teratol 2011, 91:672-681.
-
(2011)
Birt Defects Res A Clin Mol Teratol
, vol.91
, pp. 672-681
-
-
Joss-Moore, L.A.1
Wang, Y.2
Ogata, E.M.3
Sainz, A.J.4
Yu, X.5
Callaway, C.W.6
-
22
-
-
33846200332
-
Regulation of myofibroblast transdifferentiation by DNA methylation and MeCP2: implications for wound healing and fibrogenesis
-
Mann J., Oakley F., Akiboye F., Elsharkawy A., Thorne A.W., Mann D.A. Regulation of myofibroblast transdifferentiation by DNA methylation and MeCP2: implications for wound healing and fibrogenesis. Cell Death Differ 2007, 14:275-285.
-
(2007)
Cell Death Differ
, vol.14
, pp. 275-285
-
-
Mann, J.1
Oakley, F.2
Akiboye, F.3
Elsharkawy, A.4
Thorne, A.W.5
Mann, D.A.6
-
23
-
-
45849119873
-
Common variants within MECP2 confer risk of systemic lupus erythematosus
-
Sawalha A.H., Webb R., Han S., Kelly J.A., Kaufman K.M., Kimberly R.P., et al. Common variants within MECP2 confer risk of systemic lupus erythematosus. PLoS ONE 2008, 3:e1727.
-
(2008)
PLoS ONE
, vol.3
-
-
Sawalha, A.H.1
Webb, R.2
Han, S.3
Kelly, J.A.4
Kaufman, K.M.5
Kimberly, R.P.6
-
24
-
-
0006925330
-
Rett syndrome: a pervasive disorder of growth
-
Percy A., Armstrong D. Rett syndrome: a pervasive disorder of growth. Pediatr Res 1988, 23:556.
-
(1988)
Pediatr Res
, vol.23
, pp. 556
-
-
Percy, A.1
Armstrong, D.2
-
25
-
-
0022507445
-
Physical growth and development in patients with Rett syndrome
-
Holm V.A. Physical growth and development in patients with Rett syndrome. Am J Med Genet 1986, 24:119-126.
-
(1986)
Am J Med Genet
, vol.24
, pp. 119-126
-
-
Holm, V.A.1
-
26
-
-
58449117189
-
FXYD1, a modulator of Na, K-ATPase activity, facilitates female sexual development by maintaining gonadotrophin-releasing hormone neuronal excitability
-
Garcia-Rudaz C., Deng V., Matagne V., Ronnekleiv O., Bosch M., Han V., et al. FXYD1, a modulator of Na, K-ATPase activity, facilitates female sexual development by maintaining gonadotrophin-releasing hormone neuronal excitability. J Neuroendocrinol 2009, 21:108-122.
-
(2009)
J Neuroendocrinol
, vol.21
, pp. 108-122
-
-
Garcia-Rudaz, C.1
Deng, V.2
Matagne, V.3
Ronnekleiv, O.4
Bosch, M.5
Han, V.6
-
28
-
-
78650708501
-
Use of equipment and respite services and caregiver health among Australian families living with Rett syndrome
-
Urbanowicz A., Downs J., Bebbington A., Jacoby P., Girdler S., Leonard H. Use of equipment and respite services and caregiver health among Australian families living with Rett syndrome. Res Autism Spectr Disord 2011, 5:722-732.
-
(2011)
Res Autism Spectr Disord
, vol.5
, pp. 722-732
-
-
Urbanowicz, A.1
Downs, J.2
Bebbington, A.3
Jacoby, P.4
Girdler, S.5
Leonard, H.6
-
29
-
-
77957339780
-
The relationship between MECP2 mutation type and health status and service use trajectories over time in a Rett syndrome population
-
Young D., Bebbington A., de Klerk N., Bower C., Nagarajan L., Leonard H. The relationship between MECP2 mutation type and health status and service use trajectories over time in a Rett syndrome population. Res Autism Spectr Disord 2011, 5:442-449.
-
(2011)
Res Autism Spectr Disord
, vol.5
, pp. 442-449
-
-
Young, D.1
Bebbington, A.2
de Klerk, N.3
Bower, C.4
Nagarajan, L.5
Leonard, H.6
-
30
-
-
84884700682
-
-
FileMaker Inc, Santa Clara, (CA)
-
FileMaker FileMaker Server 10 2009, FileMaker Inc, Santa Clara, (CA).
-
(2009)
FileMaker FileMaker Server 10
-
-
-
32
-
-
18244387017
-
Centres for Disease Control and Prevention 2000 growth charts for the United States: improvements to the 1977 National Centre for Health Statistics version
-
Ogden C., Kuczmarski R., Flegal K., Mei Z., Guo S., Wei R., et al. Centres for Disease Control and Prevention 2000 growth charts for the United States: improvements to the 1977 National Centre for Health Statistics version. Pediatrics 2002, 109:45-60.
-
(2002)
Pediatrics
, vol.109
, pp. 45-60
-
-
Ogden, C.1
Kuczmarski, R.2
Flegal, K.3
Mei, Z.4
Guo, S.5
Wei, R.6
-
33
-
-
0033753330
-
Criteria for defenition of overweight in transition: background and recommendations for the United States
-
Kuczmarski R., Flegal K. Criteria for defenition of overweight in transition: background and recommendations for the United States. Am J Clin Nutr 2000, 72:1074-1081.
-
(2000)
Am J Clin Nutr
, vol.72
, pp. 1074-1081
-
-
Kuczmarski, R.1
Flegal, K.2
-
36
-
-
0038730163
-
-
Stata Press, College Station, TX
-
Cleves M.A., Gould W.W., Gutierrez R.G. An introduction to survival analysis using Stata 2004, Stata Press, College Station, TX. Rev. ed.
-
(2004)
An introduction to survival analysis using Stata
-
-
Cleves, M.A.1
Gould, W.W.2
Gutierrez, R.G.3
-
37
-
-
33645214414
-
Recent data on pubertal milestones in United States children: the secular trend toward earlier development
-
Herman-Giddens M. Recent data on pubertal milestones in United States children: the secular trend toward earlier development. Int J Androl 2006, 29:241-246.
-
(2006)
Int J Androl
, vol.29
, pp. 241-246
-
-
Herman-Giddens, M.1
-
38
-
-
79961167584
-
Brief report: autistic-like traits in childhood predict later age at menarche in girls
-
Whitehouse A., Mayberry M., Hickey M., Sloboda D. Brief report: autistic-like traits in childhood predict later age at menarche in girls. J Autism Dev Disord 2011, 41:1125-1130.
-
(2011)
J Autism Dev Disord
, vol.41
, pp. 1125-1130
-
-
Whitehouse, A.1
Mayberry, M.2
Hickey, M.3
Sloboda, D.4
-
39
-
-
59449088244
-
Thelarche, pubarche, and menarche attainment in children with normal and elevated body mass index
-
Rosenfield R.L., Lipton R.B., Drum M.L. Thelarche, pubarche, and menarche attainment in children with normal and elevated body mass index. Pediatrics 2009, 123:84-88.
-
(2009)
Pediatrics
, vol.123
, pp. 84-88
-
-
Rosenfield, R.L.1
Lipton, R.B.2
Drum, M.L.3
-
41
-
-
74949100523
-
Epigenetic regulation of estrogen receptor alpha gene expression in the mouse cortex during early postnatal development
-
Westberry J.M., Trout A.L., Wilson M.E. Epigenetic regulation of estrogen receptor alpha gene expression in the mouse cortex during early postnatal development. Endocrinology 2010, 151:731-740.
-
(2010)
Endocrinology
, vol.151
, pp. 731-740
-
-
Westberry, J.M.1
Trout, A.L.2
Wilson, M.E.3
-
42
-
-
67249150482
-
Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus
-
Ben-Shachar S., Chahrour M., Thaller C., Shaw C.A., Zoghbi H.Y. Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus. Hum Mol Genet 2009, 18:2431-2442.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 2431-2442
-
-
Ben-Shachar, S.1
Chahrour, M.2
Thaller, C.3
Shaw, C.A.4
Zoghbi, H.Y.5
-
43
-
-
80455173949
-
Ghrelin levels are reduced in Rett syndrome patients with eating difficulties
-
Hara M., Nishi Y., Yamashita Y., Yoh J., Takahashi S., Nagamitsu S., et al. Ghrelin levels are reduced in Rett syndrome patients with eating difficulties. Int J Dev Neurosci 2011, 29:899-902.
-
(2011)
Int J Dev Neurosci
, vol.29
, pp. 899-902
-
-
Hara, M.1
Nishi, Y.2
Yamashita, Y.3
Yoh, J.4
Takahashi, S.5
Nagamitsu, S.6
-
44
-
-
0031439378
-
The duration of puberty in girls is related to the timing of its onset
-
Marti-Henneberg C., Vizmanos B. The duration of puberty in girls is related to the timing of its onset. J Pediatr 1997, 131:618-621.
-
(1997)
J Pediatr
, vol.131
, pp. 618-621
-
-
Marti-Henneberg, C.1
Vizmanos, B.2
-
45
-
-
84858278944
-
Rett syndrome and menstruation
-
Hamilton A., Marshal M.P., Sucato G.S., Murray P.J. Rett syndrome and menstruation. J Pediatr Adolesc Gynecol 2012, 25:122-126.
-
(2012)
J Pediatr Adolesc Gynecol
, vol.25
, pp. 122-126
-
-
Hamilton, A.1
Marshal, M.P.2
Sucato, G.S.3
Murray, P.J.4
-
46
-
-
77956731272
-
Female reproductive system and bone
-
Clarke B.L., Khosla S. Female reproductive system and bone. Arch Biochem Biophys 2010, 503:118-128.
-
(2010)
Arch Biochem Biophys
, vol.503
, pp. 118-128
-
-
Clarke, B.L.1
Khosla, S.2
-
47
-
-
77951561039
-
Updating the profile of C-terminal MECP2 deletions in Rett syndrome
-
Bebbington A., Percy A., Christodoulou J., Ravine D., Ho G., Jacoby P., et al. Updating the profile of C-terminal MECP2 deletions in Rett syndrome. J Med Genet 2010, 47:242-248.
-
(2010)
J Med Genet
, vol.47
, pp. 242-248
-
-
Bebbington, A.1
Percy, A.2
Christodoulou, J.3
Ravine, D.4
Ho, G.5
Jacoby, P.6
-
48
-
-
77955755675
-
Level of purposeful hand function as a marker of clinical severity in Rett syndrome
-
Downs J., Bebbington A., Jacoby P., Williams A.M., Ghosh S., Kaufmann W.E., et al. Level of purposeful hand function as a marker of clinical severity in Rett syndrome. Dev Med Child Neurol 2010, 52:817-823.
-
(2010)
Dev Med Child Neurol
, vol.52
, pp. 817-823
-
-
Downs, J.1
Bebbington, A.2
Jacoby, P.3
Williams, A.M.4
Ghosh, S.5
Kaufmann, W.E.6
-
49
-
-
33847267187
-
Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation and the direction and degree of skewing of X-chromasome inactivation
-
Archer H., Evans J., Leonard H., Colvin L., Ravine D., Christodoulou J., et al. Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation and the direction and degree of skewing of X-chromasome inactivation. J Med Genet 2006, 44:148-152.
-
(2006)
J Med Genet
, vol.44
, pp. 148-152
-
-
Archer, H.1
Evans, J.2
Leonard, H.3
Colvin, L.4
Ravine, D.5
Christodoulou, J.6
-
50
-
-
65249169270
-
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
-
Ben Zeev B., Bebbington A., Ho G., Leonard H., de Klerk N., Gak E., et al. The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome. Neurology 2009, 72:1242-1247.
-
(2009)
Neurology
, vol.72
, pp. 1242-1247
-
-
Ben Zeev, B.1
Bebbington, A.2
Ho, G.3
Leonard, H.4
de Klerk, N.5
Gak, E.6
-
51
-
-
0019136677
-
Adolescents' self-assessment of sexual maturation
-
Duke P.M., Litt I.F., Gross R.T. Adolescents' self-assessment of sexual maturation. Pediatrics 1980, 66:918-920.
-
(1980)
Pediatrics
, vol.66
, pp. 918-920
-
-
Duke, P.M.1
Litt, I.F.2
Gross, R.T.3
-
52
-
-
0027674225
-
Validity of self-assessment of pubertal maturation in early adolescents
-
Sarni P., de Toni T., Gastaldi R. Validity of self-assessment of pubertal maturation in early adolescents. Minerva Pediatr 1993, 45:397-400.
-
(1993)
Minerva Pediatr
, vol.45
, pp. 397-400
-
-
Sarni, P.1
de Toni, T.2
Gastaldi, R.3
-
53
-
-
0036791076
-
Self-assessment of pubertal stage in overweight children
-
Bonat S., Pathomvanich A., Keil M.F., Field A.E., Yanovski J.A. Self-assessment of pubertal stage in overweight children. Pediatrics 2002, 110:743-747.
-
(2002)
Pediatrics
, vol.110
, pp. 743-747
-
-
Bonat, S.1
Pathomvanich, A.2
Keil, M.F.3
Field, A.E.4
Yanovski, J.A.5
-
54
-
-
65949084490
-
Comparison between objective assessment and self-assessment of sexual maturation in children and adolescents
-
Azevedo J.C., Brasil L.M., Macedo T.B., Pedrosa L.F., Arrais R.F. Comparison between objective assessment and self-assessment of sexual maturation in children and adolescents. J Pediatr (Rio J) 2009, 85:135-142.
-
(2009)
J Pediatr (Rio J)
, vol.85
, pp. 135-142
-
-
Azevedo, J.C.1
Brasil, L.M.2
Macedo, T.B.3
Pedrosa, L.F.4
Arrais, R.F.5
-
55
-
-
63149093112
-
Long-term plasma levels of leptin and adiponectin in Rett syndrome
-
Blardi P., de Lalla A., D'Ambrogio T., Vonella G., Ceccatelli L., Auteri A., et al. Long-term plasma levels of leptin and adiponectin in Rett syndrome. Clin Endocrinol (Oxf) 2009, 70:706-709.
-
(2009)
Clin Endocrinol (Oxf)
, vol.70
, pp. 706-709
-
-
Blardi, P.1
de Lalla, A.2
D'Ambrogio, T.3
Vonella, G.4
Ceccatelli, L.5
Auteri, A.6
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